Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion> ?p ?o ?g. }
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- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion type Assertion NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_head.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion wasGeneratedBy ECO_0000203 NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion wasDerivedFrom befree-20150227 NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion SIO_000772 24076603 NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion evidence source_evidence_literature NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.